Ortho Institute - Genetische ziekten

Orthomolekulare Bibliothek

Links to 4388 Pubmed-abstracts of human studies.
Orthomolecular selection criteria; categorized on illnesses.

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Genetische Störungen (13)

2010 - Chen F, Cao Y, [..], Cardoso WV. A retinoic acid-dependent network in the foregut controls formation of the mouse lung primordium. J Clin Invest 2010; 120(6):2040-8

2007 - Beblo S, Reinhardt H, Demmelmair H, Muntau A, Koletzko B. Effect of fish oil supplementation on fatty acid status, coordination, and fine motor skills in children with phenylketonuria. J Pediatr 2007; 150(5):479-84

2007 - Nöthlings U, Murphy SP, Wilkens LR, Henderson BE, Kolonel LN. Dietary glycemic load, added sugars, and carbohydrates as risk factors for pancreatic cancer: the Multiethnic Cohort Study. Am J Clin Nutr 2007; 86(5):1495-501

2007 - Thornalley PJ, Babaei-Jadidi R, Al Ali H, Rabbani N, Antonysunil A, Larkin J, Ahmed A, Rayman G, Bodmer CW. High prevalence of low plasma thiamine concentration in diabetes linked to a marker of vascular disease. Diabetologia 2007; 50(10):2164-70

2007 - Guldner L, Monfort C, Rouget F, Garlantezec R, Cordier S. Maternal fish and shellfish intake and pregnancy outcomes: a prospective cohort study in Brittany, France. Environ Health 2007; 6:33

2007 - Grieger JA, Nowson CA, [..], Ackland LM. Multivitamin supplementation improves nutritional status and bone quality in aged care residents. Eur J Clin Nutr 2009; 63(4):558-65

2005 - Kalpravidh RW, Wichit A, Siritanaratkul N, Fucharoen S. Effect of coenzyme Q10 as an antioxidant in beta-thalassemia/Hb E patients. Biofactors 2005; 25(1-4):225-34

2003 - Hyndman ME, Manns BJ, Snyder FF, Bridge PJ, Scott-Douglas NW, Fung E, Parsons HG. Vitamin B12 decreases, but does not normalize, homocysteine and methylmalonic acid in end-stage renal disease: a link with glycine metabolism and possible explanation of hyperhomocysteinemia in end-stage renal disease. Metabolism 2003; 52(2):168-72

2002 - Fohr IP, Prinz-Langenohl R, Brönstrup A, Bohlmann AM, Nau H, Berthold HK, Pietrzik K. 5,10-Methylenetetrahydrofolate reductase genotype determines the plasma homocysteine-lowering effect of supplementation with 5-methyltetrahydrofolate or folic acid in healthy young woman. Am J Clin Nutr 2002; 75: 275-282

2002 - Ashfield-Watt PA, Pullin CH, Whiting JM, Clark ZE, Moat SJ, Newcombe RG, Burr ML, Lewis MJ, Powers HJ, McDowell IF. Methylenetetrahydrofolate reductase 677C-->T genotype modulates homocysteine responses to a folate-rich diet or a low-dose folic acid supplement; a reandomized controlled trial. Am J Clin Nutr 2002; 76: 180-186

2002 - McNulty H, McKinley MC, Wilson B, McPartlin J, Strain JJ, Weir DG, Scott JM. Impaired functioning of thermolabile methylenetetrahydrofolate reductase is dependent on riboflavin status: implications for riboflavin requirements. Am J Clin Nutr 2002; 76(2):436-441

2001 - Musumeci O, Naini A, Slonim AE, [..], DiMauro S. Familial cerebellar ataxia with muscle coenzyme Q10 deficiency. Neurology 2001; 56(7):849-55

1999 - Ackerman M.J. et al.Swimming a gene-specific arrhytmogenic trigger for inherited long QT syndroom.Mayo Clin Proc.1999;74:1088-1094